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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18084생성일: 2026년 10월 24일

tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylate → (S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylester

https://huagongshe.com/ko/reaction/18084

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylateHCID 1502020—
반응물2-Chloro-6,7-difluoro-3-methylquinoxalineHCID 10220011—
용매DimethylformamideHCID 6228—
생성물(S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylesterHCID 86593671—

반응 조건

온도90 °C

반응 단계

(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.14 g), and 2-chloro-6,7-difluoro-3-methylquinoxaline Teng et al PCT Int. Appl (2000), WO00/42026A1 20000720 (1.14 g) were dissolved in DMF (2 ml) and heated to 90° C. for 3 days under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 10 to 50% ethyl acetate in hexane. The title compound was obtained as a pink foam (0.524 g), MH+ 393.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741329B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e387087c8a394279bd035d0d571cc60a
출처 메모uspto-grants-2010_06